Canonical Allele Identifier: PA2741888159
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2593981
ClinVar RCV Id: RCV003368829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ile2022Thr
CA1105433
NM_002016.2:c.6065T>C